Resultados de búsqueda - Hilton, Helen

Gelsolin Plays a Role in the Actin Polymerization Complex of Hair Cell Stereocilia por Mburu, Philomena, Romero, María Rosario, Hilton, Helen, Parker, Andrew, Townsend, Stuart, Kikkawa, Yoshiaki, Brown, Steve D. M.

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Atmin mediates kidney morphogenesis by modulating Wnt signaling por Goggolidou, Paraskevi, Hadjirin, Nazreen F., Bak, Aggie, Papakrivopoulou, Eugenia, Hilton, Helen, Norris, Dominic P., Dean, Charlotte H.

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Regulation of TGF-β signalling by Fbxo11, the gene mutated in the Jeff otitis media mouse mutant por Tateossian, Hilda, Hardisty-Hughes, Rachel E, Morse, Susan, Romero, Maria R, Hilton, Helen, Dean, Charlotte, Brown, Steve DM

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Analysis of the asymmetrically expressed Ablim1 locus reveals existence of a lateral plate Nodal-independent left sided signal and an early, left-right independent role for nodal f... por Stevens, Jonathan, Ermakov, Alexander, Braganca, Jose, Hilton, Helen, Underhill, Peter, Bhattacharya, Shoumo, Brown, Nigel A, Norris, Dominic P

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Loading-related regulation of gene expression in bone in the contexts of estrogen deficiency, lack of estrogen receptor α and disuse por Zaman, Gul, Saxon, Leanne K., Sunters, Andrew, Hilton, Helen, Underhill, Peter, Williams, Debbie, Price, Joanna S., Lanyon, Lance E.

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A Novel Mouse Fgfr2 Mutant, Hobbyhorse (hob), Exhibits Complete XY Gonadal Sex Reversal por Siggers, Pam, Carré, Gwenn-Aël, Bogani, Debora, Warr, Nick, Wells, Sara, Hilton, Helen, Esapa, Chris, Hajihosseini, Mohammad K., Greenfield, Andy

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Atmin modulates Pkhd1 expression and may mediate Autosomal Recessive Polycystic Kidney Disease (ARPKD) through altered non-canonical Wnt/Planar Cell Polarity (PCP) signalling por Richards, Taylor, Modarage, Kavindiya, Dean, Charlotte, McCarthy-Boxer, Aidan, Hilton, Helen, Esapa, Chris, Norman, Jill, Wilson, Patricia, Goggolidou, Paraskevi

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Pkd1l1 establishes left-right asymmetry and physically interacts with Pkd2 por Field, Sarah, Riley, Kerry-Lyn, Grimes, Daniel T., Hilton, Helen, Simon, Michelle, Powles-Glover, Nicola, Siggers, Pam, Bogani, Debora, Greenfield, Andy, Norris, Dominic P.

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Single primer amplification (SPA) of cDNA for microarray expression analysis por Smith, Lee, Underhill, Peter, Pritchard, Clare, Tymowska-Lalanne, Zuzanna, Abdul-Hussein, Saba, Hilton, Helen, Winchester, Laura, Williams, Deborah, Freeman, Tom, Webb, Sarah, Greenfield, Andy

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Haplo-Insufficiency of the Insulin Receptor in the presence of a splice-site mutation in Ppp2r2a results in a novel di-genic mouse model of type 2 diabetes por Goldsworthy, Michelle, Bai, Ying, Li, Chi-Ming, Ge, Huanying, Lamas, Edwin, Hilton, Helen, Esapa, Christopher T, Baker, Dan, Baron, Will, Juan, Todd, Véniant, Murielle M, Lloyd, David J, Cox, Roger D

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A humanized chemogenetic system inhibits murine pain-related behavior and hyperactivity in human sensory neurons por Perez-Sanchez, Jimena, Middleton, Steven J., Pattison, Luke A., Hilton, Helen, Awadelkareem, Mosab Ali, Zuberi, Sana R., Renke, Maria B., Hu, Huimin, Yang, Xun, Clark, Alex J., Smith, Ewan St. John, Bennett, David L.

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Scribble is required for normal epithelial cell–cell contacts and lumen morphogenesis in the mammalian lung por Yates, Laura L., Schnatwinkel, Carsten, Hazelwood, Lee, Chessum, Lauren, Paudyal, Anju, Hilton, Helen, Romero, M. Rosario, Wilde, Jonathan, Bogani, Debora, Sanderson, Jeremy, Formstone, Caroline, Murdoch, Jennifer N., Niswander, Lee A., Greenfield, Andy, Dean, Charlotte H.

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Upregulation of PKD1L2 provokes a complex neuromuscular disease in the mouse por Mackenzie, Francesca E., Romero, Rosario, Williams, Debbie, Gillingwater, Thomas, Hilton, Helen, Dick, Jim, Riddoch-Contreras, Joanna, Wong, Frances, Ireson, Lisa, Powles-Glover, Nicola, Riley, Genna, Underhill, Peter, Hough, Tertius, Arkell, Ruth, Greensmith, Linda, Ribchester, Richard R., Blanco, Gonzalo

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HIF–VEGF Pathways Are Critical for Chronic Otitis Media in Junbo and Jeff Mouse Mutants por Cheeseman, Michael T., Tyrer, Hayley E., Williams, Debbie, Hough, Tertius A., Pathak, Paras, Romero, Maria R., Hilton, Helen, Bali, Sulzhan, Parker, Andrew, Vizor, Lucie, Purnell, Tom, Vowell, Kate, Wells, Sara, Bhutta, Mahmood F., Potter, Paul K., Brown, Steve D. M.

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A Wars2 Mutant Mouse Model Displays OXPHOS Deficiencies and Activation of Tissue-Specific Stress Response Pathways por Agnew, Thomas, Goldsworthy, Michelle, Aguilar, Carlos, Morgan, Anna, Simon, Michelle, Hilton, Helen, Esapa, Chris, Wu, Yixing, Cater, Heather, Bentley, Liz, Scudamore, Cheryl, Poulton, Joanna, Morten, Karl J., Thompson, Kyle, He, Langping, Brown, Steve D.M., Taylor, Robert W., Bowl, Michael R., Cox, Roger D.

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ATMIN is a transcriptional regulator of both lung morphogenesis and ciliogenesis por Goggolidou, Paraskevi, L. Stevens, Jonathan, Agueci, Francesco, Keynton, Jennifer, Wheway, Gabrielle, Grimes, Daniel T., Patel, Saloni H., Hilton, Helen, Morthorst, Stine K., DiPaolo, Antonella, Williams, Debbie J., Sanderson, Jeremy, Khoronenkova, Svetlana V., Powles-Glover, Nicola, Ermakov, Alexander, Esapa, Chris T., Romero, Rosario, Dianov, Grigory L., Briscoe, James, Johnson, Colin A., Pedersen, Lotte B., Norris, Dominic P.

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Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features por Tucci, Valter, Kleefstra, Tjitske, Hardy, Andrea, Heise, Ines, Maggi, Silvia, Willemsen, Marjolein H., Hilton, Helen, Esapa, Chris, Simon, Michelle, Buenavista, Maria-Teresa, McGuffin, Liam J., Vizor, Lucie, Dodero, Luca, Tsaftaris, Sotirios, Romero, Rosario, Nillesen, Willy N., Vissers, Lisenka E.L.M., Kempers, Marlies J., Vulto-van Silfhout, Anneke T., Iqbal, Zafar, Orlando, Marta, Maccione, Alessandro, Lassi, Glenda, Farisello, Pasqualina, Contestabile, Andrea, Tinarelli, Federico, Nieus, Thierry, Raimondi, Andrea, Greco, Barbara, Cantatore, Daniela, Gasparini, Laura, Berdondini, Luca, Bifone, Angelo, Gozzi, Alessandro, Wells, Sara, Nolan, Patrick M.

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